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通过将浊点萃取在线并入化学发光池内的流动注射分析来提高样品预富集以及总血清胆红素的测定

Enhancement in sample preconcentration by the on-line incorporation of cloud point extraction to flow injection analysis inside the chemiluminescence cell and the determination of total serum bilirubin.

作者信息

Lu Chao, Song Guanqun, Lin Jin-Ming, Huie Carmen W

机构信息

State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, P.O. Box 2871, Beijing 100085, China.

出版信息

Anal Chim Acta. 2007 May 8;590(2):159-65. doi: 10.1016/j.aca.2007.03.028. Epub 2007 Mar 18.

DOI:10.1016/j.aca.2007.03.028
PMID:17448340
Abstract

The on-line incorporation of cloud point extraction (CPE) to flow injection analysis (FIA) was previously based on the use of a cotton-packed column to entrap the analyte-containing surfactant aggregates after salt-induced CPE, and then the preconcentrated analyte was eluted into a separate detection cell for subsequent chemiluminescence (CL) detection (via the peroxyoxalate CL reaction). In the work, the on-line CPE/FIA technique was improved by the following: (1) sample preconcentration and CL detection were both carried out directly inside the collection column, thus avoiding the decrease in detection sensitivity due to sample dispersion and dilution, and (2) CL detection was performed through the reaction between nitrite and hydrogen peroxide, which is compatible with aqueous samples and should allow for chemical excitation to occur more efficiently inside the collection column. In addition to more effective sample preconcentration, the CL detection of the entrapped analytes directly inside the collection column, i.e., a unique heterogeneous microenvironment in which analyte-containing surfactant aggregates were embedded within the densely packed filtering material, may also contribute to the overall increase in CL intensity (e.g., a CL enhancement factor of ca. 1000). Under optimum experimental conditions, the calibration curve was found to be linear for the CL detection of bilirubin (5 to 120 microg L(-1)), the limit of detection (S/N = 3) was 1.8 microg L(-1), and the R.S.D. was ca. 2.6% (n = 30) for 20 microg L(-1) bilirubin. Good agreements were obtained for the determination of total bilirubin in certified reference human serum samples between the present approach and an established clinical method.

摘要

此前,将浊点萃取(CPE)在线结合到流动注射分析(FIA)中是基于使用填充棉柱,在盐诱导的CPE后截留含分析物的表面活性剂聚集体,然后将预富集的分析物洗脱到单独的检测池中进行后续的化学发光(CL)检测(通过过氧草酸酯CL反应)。在这项工作中,在线CPE/FIA技术通过以下方式得到改进:(1)样品预富集和CL检测均直接在收集柱内进行,从而避免了由于样品分散和稀释导致的检测灵敏度降低;(2)CL检测通过亚硝酸盐与过氧化氢之间的反应进行,该反应与水性样品兼容,并且应能使化学激发在收集柱内更有效地发生。除了更有效的样品预富集外,在收集柱内直接对截留的分析物进行CL检测,即在一个独特的非均相微环境中,含分析物的表面活性剂聚集体嵌入紧密填充的过滤材料中,这也可能有助于CL强度的整体增加(例如,CL增强因子约为1000)。在最佳实验条件下,发现胆红素CL检测的校准曲线呈线性(5至120 μg L⁻¹),检测限(S/N = 3)为1.8 μg L⁻¹,对于20 μg L⁻¹胆红素,相对标准偏差约为2.6%(n = 30)。本方法与既定的临床方法在认证的人血清标准参考样品中总胆红素的测定方面取得了良好的一致性。

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